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Estudo do potencial antioxidante de diferentes classes de mol?culas isoladas de mel e pr?polis em c?lulas de Saccharomyces cerevisiae / Study of different molecules classes isolated from honey and propolis antioxidant activity in Saccharomyces cerevisiae cells.

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Previous issue date: 2016-08-04 / Honey and propolis are produced by bees from the nectar and sap collected from plants. In the process, the phenolic compounds derived from secondary metabolism of plants are incorporated into the products mentioned. Honey and propolis samples from multiple regions have been characterized and phenolic compounds can be divided into: hydroxybenzoic acid derivatives, hydroxycinnamic acid derivatives, flavonoids and glycosylated flavonoids. In the literature, there is no consensus among the authors about the values for in vitro antioxidant activity. Moreover, these methods do not represent physiological conditions such as concentration of substrates and metabolites interaction. The yeast Saccharomyces cerevisiae is an alternative tool for a biological assays, since it is similar to mammalian cells. The main goal of this study is to compare the antioxidant potential of different phenolic compounds classes using representatives morin, rutin, chlorogenic acid and syringic acid in control strains (BY4741) and mutant (?sod1 and ?gsh1) of S. cerevisiae. They were evaluated in dose-dependent toxicity, stress tolerance, and lipid peroxidation. All tested phenolic compounds were effective in reducing intracellular oxidative damage, especially the chlorogenic acid in the control strain. When compared to stressed cells, it promoted 75% increase on cell survival rates, compared with 57% on average for the other treatments; and 60% decrease in levels of lipid peroxidation, compared to reductions close to 47% with other treatments. In mutant strains, all compounds presented similar results. Thus, two components of the class hydroxycinnamic acid, caffeic acid and caffeic acid phenethyl ester (CAPE) were tested comparatively. Both acted as an antioxidant in S. cerevisiae, however CAPE was the most toxic substance promoting the most significant increase on reduced glutathione levels among hydroxycinnamic derivatives. This result supports some related research that claims phenolic compounds protectection is related to activation of the antioxidant system as xenobiotic action of these substances / O mel e a pr?polis s?o produzidos por abelhas, a partir da coleta de n?ctar e seiva das plantas. No processo, os compostos fen?licos oriundos do metabolismo secund?rio dos vegetais s?o incorporados aos produtos mencionados. Amostras de mel e pr?polis de diferentes regi?es foram caracterizadas e o conte?do de compostos fen?licos pode ser dividido em: derivados do ?cido hidroxibenzoico, derivados do ?cido hidroxicin?mico, flavonoides e flavonoides glicosilados. Na literatura, valores de atividade antioxidante in vitro descritos divergem consideravelmente entre os autores. Al?m disso, os m?todos in vitro (DPPH, ABTS, FRAPP, dentre outros) n?o representam condi??es fisiol?gicas como concentra??o de substratos e intera??o de metab?litos. A levedura Saccharomyces cerevisie ? uma ferramenta para ensaio biol?gico, uma vez que apresenta elevada semelhan?a com c?lulas de mam?feros superiores no sistema de defesa antioxidante. O objetivo deste trabalho foi comparar o potencial antioxidante de diferentes classes de compostos fen?licos, utilizando os representantes morina, rutina, ?cido sir?ngico e clorog?nico em cepas controle (BY4741) e mutantes (?sod1 e ?gsh1) de S. cerevisiae. Foram avaliados toxidez dose-dependente, toler?ncia ao estresse e peroxida??o lip?dica. Todos os compostos fen?licos testados foram efetivos em reduzir danos oxidativos intracelulares, com destaque para o ?cido clorog?nico na cepa controle. Quando comparado ?s c?lulas estressadas, este promoveu aumentos de 75% de sobreviv?ncia, contra 57% em m?dia dos demais tratamentos; e diminui??o de 60% em n?veis de peroxida??o lip?dica, contra redu??o pr?xima a 47% dos demais tratamentos. Nas cepas mutantes, todas as subst?ncias tiveram resultados semelhantes entre si. Desta forma, outros dois componentes da classe do ?cido hidroxicin?mico, ?cido cafeico e ?ster fenet?lico do ?cido cafeico (CAPE), foram testados comparativamente. Ambos atuaram como antioxidante em S. cerevisiae, entretanto CAPE foi a subst?ncia mais t?xica e tamb?m a que promoveu aumento mais significativo de glutationa reduzida dentre os derivados hidroxicin?micos. Esse resultado corrobora com dados de estudos que apontam que a atividade protetora dos compostos fen?licos est? relacionada a ativa??o do sistema antioxidante por a??o xenobi?tica dessas subst?ncias

Identiferoai:union.ndltd.org:IBICT/oai:localhost:jspui/1626
Date04 August 2016
CreatorsPrud?ncio, Edlene Ribeiro
ContributorsRiger, Cristiano Jorge, Salles, Cristiane Martins Cardoso de, Barbosa, Maria Ivone Martins Jacintho, Pereira, Marcos Dias
PublisherUniversidade Federal Rural do Rio de Janeiro, Programa de P?s-Gradua??o em Qu?mica, UFRRJ, Brasil, Instituto de Ci?ncias Exatas
Source SetsIBICT Brazilian ETDs
LanguagePortuguese
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Formatapplication/pdf
Sourcereponame:Biblioteca Digital de Teses e Dissertações da UFRRJ, instname:Universidade Federal Rural do Rio de Janeiro, instacron:UFRRJ
Rightsinfo:eu-repo/semantics/openAccess
Relation7. REFER?NCIAS BIBLIOGR?FICAS AMARI, F. et al. Antioxidant small molecules confer variable protection against oxidative damage in yeast mutants. Journal of Agricultural and Food Chemistry, v. 56, n. 24, p. 11740?11751, 2008. AYALA, A. et al. Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal. Oxidative Medicine and Cellular Longevity, v. 2014, p. 1?31, 2014. AZUMA, K. et al. Absorption of chlorogenic acid and caffeic acid in rats after oral administration. Journal of agricultural and food chemistry, v. 48, n. 11, p. 5496?5500, 2000. BALTRUSAITYTE, V.; VENSKUTONIS, P. R.; CEKSTERYTE, V. Radical scavenging activity of different floral origin honey and beebread phenolic extracts. Food Chemistry, v. 101, n. 2, p. 502?514, 2007. BARBOSA, K. B. F. et al. Estresse oxidativo: Conceito, implica??es e fatores modulat?rios. Revista de Nutricao, v. 23, n. 4, p. 629?643, 2010. BELINHA, I. et al. Quercetin Increases Oxidative Stress Resistance and Longevity in Saccharomyces cerevisiae. Journal of Agricultural and Food Chemistry, v. 55, p. 2446?2451, 2007. BERNT, E.; BERGMEYER, H. U. Methods of Enzymatic Analysis, Glutathione. 4. ed. Londres: Chemie Weinheim, Academic Press, 1974. BIENERT, G. P.; SCHJOERRING, J. K.; JAHN, T. P. Membrane transport of hydrogen peroxide. Biochimica et biophysica acta, v. 1758, n. 8, p. 994?1003, ago. 2006. BRASIL. Instru??o Normativa 11 de 20 de outubro de 2000. Regulamento T?cnico de Identidade e Qualidade do Mel. Dispon?vel em: <http://extranet.agricultura.gov.br/sislegis-consulta/consultarLegislacao.do?operacao=visualizar&id=7797>. BRAUER, M. J. et al. Homeostatic Adjustment and Metabolic Remodeling in Glucose-limited Yeast Cultures. Molecular Biology of the Cell, v. 16, n. 8, p. 2503?2517, 2005. BREGER, J. et al. Antifungal chemical compounds identified using a C. elegans pathogenicity assay. PLoS Pathogens, v. 3, n. 2, p. 0168?0178, 2007. 65 BRIGELIUS-FLOH?, R.; MAIORINO, M. Glutathione peroxidases. Biochimica et Biophysica Acta - General Subjects, v. 1830, n. 5, p. 3289?3303, 2013. B?FALO, M. C.; SFORCIN, J. M. The modulatory effects of caffeic acid on human monocytes and its involvement in propolis action. Journal of Pharmacy and Pharmacology, v. 67, n. 5, p. 740?745, 2015. CAI, Y. et al. Structure-radical scavenging activity relationships of phenolic compounds from traditional Chinese medicinal plants. Life sciences, v. 78, n. 25, p. 2872?2888, 2006. CALLEMIEN, D.; COLLIN, S. Structure, Organoleptic Properties, Quantification Methods, and Stability of Phenolic Compounds in Beer?A Review. Food Reviews International, v. 26, n. June 2014, p. 1?84, 2009. CAN, Z. et al. An investigation of Turkish honeys: Their physico-chemical properties, antioxidant capacities and phenolic profiles. Food Chemistry, v. 180, p. 133?141, 2015. CARILLON, J. et al. Superoxide dismutase administration, a potential therapy against oxidative stress related diseases: Several routes of supplementation and proposal of an original mechanism of action. Pharmaceutical Research, v. 30, n. 11, p. 2718?2728, 2013. CARLOS, J. et al. Antimicrobial activity , phenolic profile and role in the inflammation of propolis. Food and Chemical Toxicology, v. 50, p. 1790?1795, 2012. CELIK, S.; ERDOGAN, S. Caffeic acid phenethyl ester (CAPE) protects brain against oxidative stress and inflammation induced by diabetes in rats. Molecular and Cellular Biochemistry, v. 312, n. 1-2, p. 39?46, 2008. CELLI, N. et al. In vitro and in vivo stability of caffeic acid phenethyl ester, a bioactive compound of propolis. Journal of Agricultural and Food Chemistry, v. 55, n. 9, p. 3398?3407, 2007. CHEN, F.; GONG, P. Caffeic acid phenethyl ester protect mice hepatic damage against Cadmium exposure. Procedia Environmental Sciences, v. 8, p. 633?636, 2011. CIGUT, T. et al. Antioxidative activity of propolis extract in yeast cells. Journal of Agricultural and Food Chemistry, v. 59, n. 21, p. 11449?11455, 2011. COELHO, V. R. et al. Antiepileptogenic, antioxidant and genotoxic evaluation of rosmarinic acid and its metabolite caffeic acid in mice. Life Sciences, v. 122, p. 65?71, 2015. COSTA, V.; MORADAS-FERREIRA, P. Oxidative stress and signal transduction in 66 Saccharomyces cerevisiae: Insights into ageing, apoptosis and diseases. Molecular Aspects of Medicine, v. 22, n. 4-5, p. 217?246, 2001. CRUZ, M. A. O. Evaluation and characterization of antioxidant and antigenotoxic properties of Portuguese propolis. [s.l: s.n.]. DA SILVA, C. G. et al. Protective effects of flavonoids and extract from Vellozia kolbekii Alves against oxidative stress induced by hydrogen peroxide in yeast. Journal of Natural Medicines, v. 66, n. 2, p. 367?372, 2012. DA SILVA, I. A. A. et al. Phenolic profile, antioxidant activity and palynological analysis of stingless bee honey from Amazonas, Northern Brazil. Food chemistry, v. 141, n. 4, p. 3552?8, 15 dez. 2013. DA SILVA, P. M. et al. Honey: Chemical composition, stability and authenticity. Food Chemistry, v. 196, p. 309?323, 2016. DANI, C. et al. Antioxidant protection of resveratrol and catechin in Saccharomyces cerevisiae. Journal of Agricultural and Food Chemistry, v. 56, n. 11, p. 4268?4272, 2008. DEMIDCHIK, V. Mechanisms of oxidative stress in plants: From classical chemistry to cell biology. Environmental and Experimental Botany, v. 109, p. 212?228, jul. 2014. EL-SEEDI, H. R. et al. Biosynthesis, natural sources, dietary intake, pharmacokinetic properties, and biological activities of hydroxycinnamic acids. Journal of Agricultural and Food Chemistry, v. 60, n. 44, p. 10877?10895, 2012. ETERAF-OSKOUEI, T.; NAJAFI, M. Traditional and modern uses of natural honey in human diseases: A review. Iranian Journal of Basic Medical Sciences, v. 16, n. 6, p. 731?742, 2013. FARAH, A.; DUARTE, G. Bioavailability and Metabolism of Chlorogenic Acids from Coffee. [s.l.] Elsevier Inc., 2015. FENG, R. et al. Inhibition of activator protein-1, NF-??B, and MAPKs and induction of phase 2 detoxifying enzyme activity by chlorogenic acid. Journal of Biological Chemistry, v. 280, n. 30, p. 27888?27895, 2005. FERNANDES, P. N. et al. Oxidative stress response in eukaryotes: effect of glutathione, superoxide dismutase and catalase on adaptation to peroxide and menadione stresses in Saccharomyces cerevisiae. Redox report : communications in free radical research, v. 12, 67 n. 5, p. 236?244, 2007. FROZZA, C. O. DA S. et al. Chemical characterization, antioxidant and cytotoxic activities of Brazilian red propolis. Food and Chemical Toxicology, v. 52, p. 137?142, 2013. GA?I?, U. et al. Phenolic profile and antioxidant activity of Serbian polyfloral honeys. Food Chemistry, v. 145, p. 599?607, 2014. GIACOMETTI MUHVI, D., PAVLETI, A., DUDARI, L., J. Cocoa polyphenols exhibit antioxidant, anti-inflammatory, anticancerogenic, and anti-necrotic activity in carbon tetrachloride-intoxicated mice. Journal of Functional Foods, v. 23, p. 177?187, 2016. G??ER, H.; G?L?IN, I. Caffeic acid phenethyl ester (CAPE): correlation of structure and antioxidant properties. International journal of food sciences and nutrition, v. 62, n. 8, p. 821?5, 2011. GONTHIER, M. P. et al. Microbial metabolism of caffeic acid and its esters chlorogenic and caftaric acids by human faecal microbiota in vitro. Biomedicine and Pharmacotherapy, v. 60, n. 9, p. 536?540, 2006. GOSTIMSKAYA, I.; GRANT, C. M. Yeast mitochondrial glutathione is an essential antioxidant with mitochondrial thioredoxin providing a back-up system. Free Radical Biology and Medicine, v. 94, p. 55?65, 2016. GRANT, C. M.; MACIVER, F. H.; DAWES, I. W. Mitochondrial function is required for resistance to oxidative stress in the yeast Saccharomyces cerevisiae. FEBS Letters, v. 410, n. 2-3, p. 219?222, 1997. GREGORIS, E.; STEVANATO, R. Correlations between polyphenolic composition and antioxidant activity of Venetian propolis. Food and Chemical Toxicology, v. 48, n. 1, p. 76?82, 2010. HABIB, H. M. et al. Bioactive components, antioxidant and DNA damage inhibitory activities of honeys from arid regions. Food chemistry, v. 153, p. 28?34, 15 jun. 2014. HERMAN, P. K. Stationary phase in yeast. Current Opinion in Microbiology, v. 5, n. 6, p. 602?607, 2002. IMLAY, J. A. The molecular mechanisms and physiological consequences of oxidative stress: lessons from a model bacterium. Nature reviews. Microbiology, v. 11, n. 7, p. 443?54, 2013. ITOH, A. et al. Hepatoprotective Effect of Syringic Acid and Vanillic Acid on CCl 4 - 68 Induced Liver Injury. Biological & pharmaceutical bulletin, v. 33, n. 6, p. 983?987, 2010. JENSEN, S. J. K. Oxidative stress and free radicals. Journal of Molecular Structure: THEOCHEM, v. 666-667, p. 387?392, 2003. KECKE?, S. et al. The determination of phenolic profiles of Serbian unifloral honeys using ultra-high-performance liquid chromatography/high resolution accurate mass spectrometry. Food Chemistry, v. 138, n. 1, p. 32?40, 2013. KIM, J.; LEE, K. W. Coffee and its Active Compounds are Neuroprotective. Coffee in Health and Disease Prevention, p. 423?427, 2015. KONISHI, Y.; KOBAYASHI, S. Transepithelial Transport of Cholorogenic Acid, Caffeic Acid, and Their Colonic Metabolites in Intestinal Caco-2 Cell Monolayers. J. Agric. Food Chem, v. 52, p. 2518?2526, 2004. KRISHNAIAH, D.; SARBATLY, R.; NITHYANANDAM, R. A review of the antioxidant potential of medicinal plant species. Food and Bioproducts Processing, v. 89, n. 3, p. 217?233, 2011. LAMBERT, J. D.; ELIAS, R. J. The antioxidant and pro-oxidant activities of green tea polyphenols: A role in cancer prevention. Archives of Biochemistry and Biophysics, v. 501, n. 1, p. 65?72, 2010. LAVOV?, B. et al. Diauxic growth of Saccharomyces cerevisiae. Journal of Microbiology,Biotechnology and Food Sciences, n. 2002, p. 122?123, 2014. LE?N-GONZ?LEZ, A. J.; AUGER, C.; SCHINI-KERTH, V. B. Pro-oxidant activity of polyphenols and its implication on cancer chemoprevention and chemotherapy. Biochemical Pharmacology, v. 98, n. 3, p. 371?380, 2015. LI, S. et al. Research progress of natural antioxidants in foods for the treatment of diseases. Food Science and Human Wellness, dez. 2014. LIMA, ?. S.; SAES, D.; ABDALLA, P. Peroxida??o lip?dica : mecanismos e avalia??o em amostras biol?gicas. Revista Brasileira de Ci?ncias Farmac?uticas, v. 37, n. 3, p. 293?303, 2001. LOUREIRO, A. P. M.; DI, P.; MEDEIROS, M. H. G. Forma??o de adutos exoc?clicoscom bases de DNA:Implica??es em mutagenese e carcinog?nese. Qu?mica Nova, v. 25, n. 5, p. 777?793, 2002. 69 LOZANO, R. et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: A systematic analysis for the Global Burden of Disease Study 2010. The Lancet, v. 380, n. 9859, p. 2095?2128, 2012. LUSHCHAK, V. I. Budding yeast Saccharomyces cerevisiae as a model to study oxidative modification of proteins in eukaryotesActa Biochimica Polonica, 2006. LUSHCHAK, V. I. Oxidative stress in yeast. Biochemistry. Biokhimiia, v. 75, n. 3, p. 281?296, 2010. LUSHCHAK, V. I. Free radicals, reactive oxygen species, oxidative stress and its classification. Chemico-Biological Interactions, v. 224, p. 164?175, 2014. MAETA, K. et al. Green tea polyphenols function as prooxidants to activate oxidative-stress-responsive transcription factors in yeasts. Applied and Environmental Microbiology, v. 73, n. 2, p. 572?580, 2007. MANDALARI, G. et al. Antimicrobial activity of flavonoids extracted from bergamot (Citrus bergamia Risso) peel, a byproduct of the essential oil industry. Journal of Applied Microbiology, v. 103, n. 6, p. 2056?2064, 2007. MANFREDINI, V. et al. Glutathione peroxidase induction protects Saccharomyces cerevisiae sod1? sod2? double mutants against oxidative damage. Brazilian Journal of Medical and Biological Research, v. 37, n. 2, p. 159?165, 2004. MAR?O, P. H.; POPPI, R. J.; SCARMINIO, I. S. Procedimentos anal?ticos para identifica??o de antocianinas presentes em extratos naturais. Quimica Nova, v. 31, n. 5, p. 1218?1223, 2008. MARCUCCI, M. C. Biological and therapeutic properties of chemical propolis constituents. Quimica Nova, v. 19, n. 5, p. 529?536, 1996. MARIANI, D. et al. Involvement of glutathione transferases, Gtt1and Gtt2, with oxidative stress response generated by H2O2 during growth of Saccharomyces cerevisiae. Redox Report, v. 13, n. 6, p. 246?254, 2008. MASUOKA, N.; MATSUDA, M.; KUBO, I. Characterisation of the antioxidant activity of flavonoids. Food Chemistry, v. 131, n. 2, p. 541?545, 2012. MAURYA, D. K.; DEVASAGAYAM, T. P. A. Antioxidant and prooxidant nature of hydroxycinnamic acid derivatives ferulic and caffeic acids. Food and Chemical Toxicology, 70 v. 48, n. 12, p. 3369?3373, 2010. MENDOZA-WILSON, A. M.; SANTACRUZ-ORTEGA, H.; BALANDR?N-QUINTANA, R. R. Relationship between structure, properties, and the radical scavenging activity of morin. Journal of Molecular Structure, v. 995, n. 1-3, p. 134?141, 2011. MORGAN, B. et al. Multiple glutathione disulfide removal pathways mediate cytosolic redox homeostasis. Nat Chem Biol, v. 9, n. 2, p. 119?125, 2013. MURTAZA, G.; KARIM, S.; AKRAM, M. Caffeic Acid Phenethyl Ester and Therapeutic Potentials. BioMed Research International, v. 2014, p. 1?9, 2014. NELSON, D. L.; COX, M. M. Princ?pios de Bioqu?mica de Lehninger. 6a. ed. [s.l.] Artmed, 2014. v. 2 NELSON, S. K. et al. The induction of human superoxide dismutase and catalase in vivo: A fundamentally new approach to antioxidant therapy. Free Radical Biology and Medicine, v. 40, n. 2, p. 341?347, 2006. ORINO, K. et al. Ferritin and the response to oxidative stress. The Biochemical journal, v. 357, n. Pt 1, p. 241?247, 2001. OSAWA, C. C.; DE FEL?CIO, P. E.; GON?ALVES, L. A. G. Teste de TBA aplicado a carnes e derivados: M?todos tradicionais, modificados e alternativos. Quimica Nova, v. 28, n. 4, p. 655?663, 2005. PEREIRA, M. D. et al. Targets of oxidative stress in yeast sod mutants. Biochimica et Biophysica Acta, v. 1620, n. 1-3, p. 245?251, 2003. PEREIRA, M. D.; ELEUTHERIO, E. C.; PANEK, A. D. Acquisition of tolerance against oxidative damage in Saccharomyces cerevisiae. BMC microbiology, v. 1, p. 11, 2001. PROCH?ZKOV?, D.; BOU?OV?, I.; WILHELMOV?, N. Antioxidant and prooxidant properties of flavonoids. Fitoterapia, v. 82, n. 4, p. 513?523, 2011. RAO, P. V. et al. Biological and therapeutic effects of honey produced by honey bees and stingless bees: a comparative review. Revista Brasileira de Farmacognosia, p. 1?8, 2016. REGINATO, F. F. Z.; DA SILVA, A. R. H.; BAUERMANN, L. D. F. Avalia??o do uso de flavonoides no tratamento da inflama??o. Revista Cubana de Farmacia, v. 49, n. 3, p. 569?582, 2015. ROLEIRA, F. M. F. et al. Plant derived and dietary phenolic antioxidants: Anticancer 71 properties. Food Chemistry, v. 183, p. 235?258, 2015. S?, R. A. DE et al. Brazilian propolis protects Saccharomyces cerevisiae cells against oxidative stress. Brazilian journal of microbiology, v. 44, n. 3, p. 993?1000, 2013. SADOWSKA-BARTOSZ, I. et al. Dimethyl sulfoxide induces oxidative stress in the yeast Saccharomyces cerevisiae. FEMS yeast research, v. 13, n. 8, p. 820?30, 2013. SALGUEIRO, F. B. et al. Phenolic Composition and antioxidant proprieties of brasilian honeys. Qu?mica Nova, v. 37, n. 5, p. 821?826, 2014. SATO, Y. et al. In vitro and in vivo antioxidant properties of chlorogenic acid and caffeic acid. International Journal of Pharmaceutics, 2011. SETHIYA, N. K.; TRIVEDI, A.; MISHRA, S. The total antioxidant content and radical scavenging investigation on 17 phytochemical from dietary plant sources used globally as functional food. Biomedicine & Preventive Nutrition, v. 4, n. 3, p. 439?444, jul. 2014. SHAHIDI, F.; AMBIGAIPALAN, P. Phenolics and polyphenolics in foods, beverages and spices: Antioxidant activity and health effects - A review. Journal of Functional Foods, v. 18, p. 820?897, 2015. SILVA, J. A. et al. Aplica??o da metodologia de planejamento fatorial e an?lise de superf?cies de resposta para otimiza??o da fermenta??o alco?lica. Quimica Nova, v. 31, n. 5, p. 1073?1077, 2008. SILVA, R. et al. Flavon?ides: constitui??o qu?mica, a??es medicinais e potencial t?xico. Acta toxicol?gica argentina, v. 23, p. 36?43, 2015. SOARES, D. G.; ANDREAZZA, A. C.; SALVADOR, M. Avalia??o de compostos com atividade antioxidante em c?lulas da levedura Saccharomyces cerevisiae. Revista Brasileira de Ci?ncias Farmac?uticas, v. 41, n. 1, p. 95?100, 2005. SOARES, S. E. ?cidos fen?licos como antioxidantes Phenolic acids as antioxidants. Revista de Nutri??o, v. 15, n. 1, p. 71?81, 2002. SOUSA, C. M. D. M. et al. Fen?is totais e atividade antioxidante de cinco plantas medicinais. Quimica Nova, v. 30, n. 2, p. 351?355, 2007. SOUSA, J. M. et al. Polyphenolic profile and antioxidant and antibacterial activities of monofloral honeys produced by Meliponini in the Brazilian semiarid region. Food Research International, v. 84, p. 61?68, 2016. 72 SOVA, M. Antioxidant and antimicrobial activities of cinnamic acid derivatives. Mini reviews in medicinal chemistry, v. 12, n. 8, p. 749?67, 2012. SREEDHARAN, V.; VENKATACHALAM, K. K.; NAMASIVAYAM, N. Effect of morin on tissue lipid peroxidation and antioxidant status in 1, 2-dimethylhydrazine induced experimental colon carcinogenesis. Investigational New Drugs, v. 27, n. 1, p. 21?30, 2009. STEELS, E. L.; LEARMONTH, R. P.; WATSON, K. Stress tolerance and membrane lipid unsaturation in Saccharomyces cerevisiae grown aerobically or anaerobically. Microbiology (Reading, England), v. 140 ( Pt 3, n. 1994, p. 569?76, 1994. ST?PNIAK, J.; LEWI?SKI, A.; KARBOWNIK-LEWI?SKA, M. Membrane lipids and nuclear DNA are differently susceptive to Fenton reaction substrates in porcine thyroid. Toxicology in vitro, v. 27, n. 1, p. 71?8, fev. 2013. SUN, K. et al. Anti-Aging Effects of Hesperidin on Saccharomyces cerevisiae via Inhibition of Reactive Oxygen Species and UTH1 Gene Expression. Bioscience, Biotechnology, and Biochemistry, v. 76, n. 4, p. 640?645, 2012. TOHAMY, A. A. et al. Assessment of anti-mutagenic, anti-histopathologic and antioxidant capacities of Egyptian bee pollen and propolis extracts. Cytotechnology, v. 66, n. 2, p. 283?297, 2014. TOLEDANO, M. B. et al. Oxidative stress responses in yeast. Yeast Stress Responses, v. 1, p. 242?87, 2003. TREUSCH, S. et al. Functional links between A? toxicity, endocytic trafficking, and Alzheimer?s disease risk factors in yeast. Science (New York, N.Y.), v. 334, n. 6060, p. 1241?5, 2011. VALENZUELA-BARRA, G. et al. Anti-inflammatory activity and phenolic profile of propolis from two locations in Regi??n Metropolitana de Santiago, Chile. Journal of Ethnopharmacology, v. 168, p. 37?44, 2015. VALKO, M. et al. Free radicals and antioxidants in normal physiological functions and human disease. The international journal of biochemistry & cell biology, v. 39, n. 1, p. 44?84, 2007. VAN RAAMSDONK, J. M.; HEKIMI, S. From the Cover: Superoxide dismutase is dispensable for normal animal lifespan. Proceedings of the National Academy of Sciences, v. 109, n. 15, p. 5785?5790, 2012. 73 VANDAMME, L. et al. Honey in modern wound care: A systematic review. Burns, v. 39, n. 8, p. 1514?1525, 2013. VENU GOPAL, J. Morin Hydrate: Botanical origin, pharmacological activity and its applications: A mini-review. Pharmacognosy Journal, v. 5, n. 3, p. 123?126, 2013. VILLA?O, D. et al. Radical scavenging ability of polyphenolic compounds towards DPPH free radical. Talanta, v. 71, n. 1, p. 230?235, 2007. VIUDA-MARTOS, M. et al. Functional properties of honey, propolis, and royal jelly. Journal of food science, v. 73, n. 9, p. R117?24, nov. 2008. WILMSEN, P. K.; SPADA, D. S.; SALVADOR, M. Antioxidant activity of the flavonoid hesperidin in chemical and biological systems. Journal of Agricultural and Food Chemistry, v. 53, n. 12, p. 4757?4761, 2005. WU, M. J. et al. An antioxidant screening assay based on oxidant-induced growth arrest in Saccharomyces cerevisiae. FEMS Yeast Research, v. 11, n. 4, p. 379?387, 2011. WU, W. M. et al. Free radical scavenging and antioxidative activities of caffeic acid phenethyl ester (CAPE) and its related compounds in solution and membranes: A structure-activity insight. Food Chemistry, v. 105, n. 1, p. 107?115, 2007. XIANG, L. et al. Anti-aging effects of phloridzin, an apple polyphenol, on yeast via the SOD and Sir2 genes. Bioscience, biotechnology, and biochemistry, v. 75, n. 5, p. 854?858, 2011. XIANG, Z. N.; NING, Z. X. Scavenging and antioxidant properties of compound derived from chlorogenic acid in South-China honeysuckle. LWT - Food Science and Technology, v. 41, n. 7, p. 1189?1203, 2008. YANG, J.; GUO, J.; YUAN, J. In vitro antioxidant properties of rutin. LWT - Food Science and Technology, v. 41, n. 6, p. 1060?1066, 2008. YE, Z.-W. et al. Oxidative stress, redox regulation and diseases of cellular differentiation. Biochimica et Biophysica Acta (BBA) - General Subjects, v. 1850, n. 8, p. 1607?1621, 2014. YEN, G.-C. et al. Pro-oxidative properties of flavonoids in human lymphocytes. Bioscience, biotechnology, and biochemistry, v. 67, n. 6, p. 1215?1222, 2003. ZHANG, H. et al. Inhibitory Properties of Aqueous Ethanol Extracts of Propolis on Alpha-Glucosidase. Evidence-Based Complementary and Alternative Medicine, v. 2015, p. 1?7, 74 2015a. ZHANG, Y. et al. Assessment of the correlations between reducing power, scavenging DPPH activity and anti-lipid-oxidation capability of phenolic antioxidants. LWT - Food Science and Technology, v. 63, n. 1, p. 569?574, 2015b. ZYRACKA, E. et al. Yeast as a biosensor for antioxidants: Simple growth tests employing a Saccharomyces cerevisiae mutant defective in superoxide dismutase. Acta Biochimica Polonica, v. 52, n. 3, p. 679?684, 2005.

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